OXFENDAZOLE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	UNKNOWN
Molecular Formula	C15H13N3O3S
Molecular Weight	315.347
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of OXFENDAZOLE

Structure Search

SMILES

COC(=O)NC1=NC2=CC=C(C=C2N1)[S+]([O-])C3=CC=CC=C3

InChI

InChIKey=BEZZFPOZAYTVHN-UHFFFAOYSA-N

InChI=1S/C15H13N3O3S/c1-21-15(19)18-14-16-12-8-7-11(9-13(12)17-14)22(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)

HIDE SMILES / InChI

Molecular Formula	C15H13N3O3S
Molecular Weight	315.347
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:16:45 UTC 2023` Edited by `admin` on `Fri Dec 15 15:16:45 UTC 2023`
Record UNII	OMP2H17F9E
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

OXFENDAZOLE

Official Name

English

OXFENDAZOLE [USAN]

Common Name

English

OXFENDAZOLE [USP MONOGRAPH]

Common Name

English

oxfendazole [INN]

Common Name

English

CARBAMIC ACID, 5-(PHENYLSULFINYL)-1H-BENZIMIDAZOL-2-YL-, METHYL ESTER

Common Name

English

OXFENDAZOLE [MART.]

Common Name

English

OXFENDAZOLE [GREEN BOOK]

Common Name

English

RS-8858

Code

English

SYNANTHIC

Brand Name

English

OXFENDAZOLE [MI]

Common Name

English

NSC-758943

Code

English

Methyl 5-(phenylsulfinyl)-2-benzimidazolecarbamate

Common Name

English

OXFENDAZOLE [USP-RS]

Common Name

English

Classification Tree Code System Code

CFR

21 CFR 556.495

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

CFR

21 CFR 520.1631

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

NCI_THESAURUS

C250

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

CFR

21 CFR 520.1628

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

FDA ORPHAN DRUG

597217

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

CFR

21 CFR 520.1629

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

WHO-VATC

QP52AC02

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

CFR

21 CFR 520.1630

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

FDA ORPHAN DRUG

435514

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

WHO-VATC

QP52AC52

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

Code System Code Type Description

PUBCHEM

40854

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

RXCUI

32634

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

RxNorm

SMS_ID

100000083039

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

NSC

758943

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

INN

3853

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

WIKIPEDIA

Oxfendazole

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

EPA CompTox

DTXSID9044112

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

CAS

53716-50-0

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

DAILYMED

OMP2H17F9E

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

MERCK INDEX

m8304

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

Merck Index

MESH

C011030

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

NCI_THESAURUS

C75229

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

FDA UNII

OMP2H17F9E

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

RS_ITEM_NUM

1483301

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

ChEMBL

CHEMBL42442

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

ECHA (EC/EINECS)

258-714-5

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

DRUG BANK

DB11446

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

EVMPD

SUB09519MIG

Created by admin on Fri Dec 15 15:16:45 UTC 2023 , Edited by admin on Fri Dec 15 15:16:45 UTC 2023

PRIMARY

Related Record Type Details


					OMP2H17F9E

BASIS OF STRENGTH->SUBSTANCE

Interaction Type:

ASSAY (TITRATION)

Qualification:

EP

Amount:


					OMP2H17F9E

BASIS OF STRENGTH->SUBSTANCE

Interaction Type:

ASSAY (TITRATION)

Qualification:

USP

Amount:

Related Record Type Details


					FQM8UA6SPQ

OXFENDAZOLE SULFONE

METABOLITE -> PARENT

Amount:

Related Record Type Details


					621BVT9M36

IMPURITY -> PARENT

Comments:

from Standard solution 1(Dissolve a quantity of USP Oxfendazole RS in Diluent to obtain a solution having a concentration of 0.1 mg per mL)

Interaction Type:

CHROMATOGRAPHIC PURITY (TLC)

Qualification:

USP

Amount:


					FQM8UA6SPQ

OXFENDAZOLE SULFONE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					621BVT9M36

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					ZR38Z38HB3

5-(PHENYLSULFINYL)-1H-BENZIMIDAZOL-2-AMINE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					0WWM0PC8OB

N,N'-BIS(5-(PHENYLSULFINYL)-1H-BENZIMIDAZOL-2-YL)UREA

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					621BVT9M36

IMPURITY -> PARENT

Comments:

from Standard solution 2 (Dissolve a quantity of USP Fenbendazole RS in Diluent to obtain a solution having a concentration of 0.05 mg per mL)

Interaction Type:

CHROMATOGRAPHIC PURITY (TLC)

Qualification:

USP

Amount:

Related Record Type Details


					OMP2H17F9E

ACTIVE MOIETY